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- [21] Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disordersScientific Reports, 8Danijela Krgovic论文数: 0 引用数: 0 h-index: 0机构: University Medical Centre Maribor,Laboratory of Medical GeneticsNadja Kokalj Vokac论文数: 0 引用数: 0 h-index: 0机构: University Medical Centre Maribor,Laboratory of Medical GeneticsAndreja Zagorac论文数: 0 引用数: 0 h-index: 0机构: University Medical Centre Maribor,Laboratory of Medical GeneticsHojka Gregoric Kumperscak论文数: 0 引用数: 0 h-index: 0机构: University Medical Centre Maribor,Laboratory of Medical Genetics
- [22] Incorporating Gene-Environment Interaction in Testing for Association with Rare Genetic VariantsHUMAN HEREDITY, 2014, 78 (02) : 81 - 90Chen, Han论文数: 0 引用数: 0 h-index: 0机构: Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USA Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USAMeigs, James B.论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Gen Med, Boston, MA USA Harvard Univ, Sch Med, Dept Med, Boston, MA USA Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USADupuis, Josee论文数: 0 引用数: 0 h-index: 0机构: Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USA NHLBI, Framingham Heart Study, Framingham, MA USA Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USA
- [23] Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disordersMOLECULAR PSYCHIATRY, 2014, 19 (08) : 872 - 879Kenny, E. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandCormican, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandFurlong, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandKenny, E. Heron G.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandFahey, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandKelleher, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandEnnis, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Coll Dublin, Sch Med & Med Sci, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandTropea, D.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandAnney, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandCorvin, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandDonohoe, G.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandGallagher, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandGill, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, IrelandMorris, D. W.论文数: 0 引用数: 0 h-index: 0机构: Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Univ Dublin Trinity Coll, Inst Mol Med, Dept Psychiat, Neuropsychiat Genet Res Grp, Dublin 2, Ireland
- [24] Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disordersMolecular Psychiatry, 2014, 19 : 872 - 879E M Kenny论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryP Cormican论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryS Furlong论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryE Heron论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryG Kenny论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryC Fahey论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryE Kelleher论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryS Ennis论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryD Tropea论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryR Anney论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryA P Corvin论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryG Donohoe论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryL Gallagher论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryM Gill论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryD W Morris论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of Psychiatry
- [25] Distortion of the normal function of synaptic cell adhesion molecules by genetic variants as a risk for autism spectrum disordersBRAIN RESEARCH BULLETIN, 2017, 129 : 82 - 90Baig, Deeba Noreen论文数: 0 引用数: 0 h-index: 0机构: Forman Christian Coll, Dept Biol Sci, Zahoor Elahi Rd, Lahore 54600, Pakistan Forman Christian Coll, Dept Biol Sci, Zahoor Elahi Rd, Lahore 54600, PakistanYanagawa, Toru论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Fac Med, Dept Oral & Maxillofacial Surg, Ibaraki 3058575, Japan Forman Christian Coll, Dept Biol Sci, Zahoor Elahi Rd, Lahore 54600, PakistanTabuchi, Katsuhiko论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Mol & Cellular Physiol, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Inst Biomed Sci Interdisciplinary Cluster Cutting, Matsumoto, Nagano 3908621, Japan JST, PRESTO, Saitama 3320012, Japan Forman Christian Coll, Dept Biol Sci, Zahoor Elahi Rd, Lahore 54600, Pakistan
- [26] Investigating the role of rare genetic variants of GP6 gene in platelet functionLANCET, 2014, 383 : 74 - 74Mitrofan, Claudia-Gabriela论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Med, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med, Cambridge CB2 0QQ, EnglandHansen, Sjoert论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Haematol, NHS Blood & Transplant, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med, Cambridge CB2 0QQ, EnglandSmethurst, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Dept Haematol, NHS Blood & Transplant, Cambridge CB2 0QQ, England Univ Cambridge, Dept Med, Cambridge CB2 0QQ, England论文数: 引用数: h-index:机构:
- [27] Whole exome sequencing followed by reverse phenotyping in patients with neurodevelopmental disorders identifies rare genetic syndromes and reveals novel clinical and genetic variantsEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 485 - 486论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Avdjieva-Tzavella, Daniela论文数: 0 引用数: 0 h-index: 0机构: Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, BulgariaPeycheva, Valentina论文数: 0 引用数: 0 h-index: 0机构: Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, Bulgaria Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, BulgariaLitvinenko, Ivan论文数: 0 引用数: 0 h-index: 0机构: SBAL Childrens Hosp Prof Dr Ivan Mitev, Neurol Clin, Sofia, Bulgaria Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, BulgariaTacheva, Genoveva论文数: 0 引用数: 0 h-index: 0机构: SBAL Childrens Hosp Prof Dr Ivan Mitev, Pediat, Sofia, Bulgaria Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, BulgariaAleksandrova, Iliyana论文数: 0 引用数: 0 h-index: 0机构: Med Univ Sofia, Children Neurol Clin, Univ Hosp Neurol & Psychiat Sveti Naum, Sofia, Bulgaria Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, BulgariaGuergelcheva, Velina论文数: 0 引用数: 0 h-index: 0机构: UMBAL Sofiamed, Neurol Clin, Sofia, Bulgaria Sofia Univ St Kliment Ochridski, Med Fac, Sofia, Bulgaria Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, BulgariaBojinova-Tchamova, Veneta论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Neurol & Psychiat Sveti Naum, Children Neurol Clin, Sofia, Bulgaria Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, BulgariaMitev, Vanyo论文数: 0 引用数: 0 h-index: 0机构: Med Univ Sofia, Med Chem & Biochem, Sofia, Bulgaria Med Univ Sofia, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, Bulgaria论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [28] Shared rare genetic variants in multiplex autism families suggest a social memory gene under selectionSCIENTIFIC REPORTS, 2025, 15 (01):Lee, Kang Seon论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaLee, Taeyeop论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Daejeon 34141, South Korea Univ Ulsan, Asan Med Ctr, Dept Psychiat, Coll Med, Seoul 05505, South Korea Asan Med Ctr, Asan Inst Life Sci, Translat Biomed Res Grp, Seoul 05505, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaKim, Mujun论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaIgnatova, Elizaveta论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaBan, Hyo-Jeong论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaSung, Min Kyung论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaKim, Younghoon论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaKim, Youn-Jae论文数: 0 引用数: 0 h-index: 0机构: Natl Canc Ctr, Specif Organs Canc Branch, Goyang 10408, Gyeonggi, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaHan, Jin-Hee论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South KoreaChoi, Jung Kyoon论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea
- [29] SHARED RARE GENETIC VARIANTS IN MULTIPLEX AUTISM FAMILIES SUGGEST A SOCIAL MEMORY GENE UNDER SELECTIONEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2024, 87 : 239 - 239Lee, Taeyeop论文数: 0 引用数: 0 h-index: 0机构: Asan Med Ctr, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaLee, Kang Seon论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaKim, Mujun论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaIgnatova, Elizaveta论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaBan, Hyo-Jeong论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaSung, Min Kyung论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaKim, Younghoon论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaKim, Youn-Jae论文数: 0 引用数: 0 h-index: 0机构: Natl Canc Ctr, Goyang, South Korea Asan Med Ctr, Seoul, South KoreaHan, Jin-Hee论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South KoreaChoi, Jung Kyoon论文数: 0 引用数: 0 h-index: 0机构: Korea Adv Inst Sci & Technol, Seoul, South Korea Asan Med Ctr, Seoul, South Korea
- [30] Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traitsNATURE GENETICS, 2025, 57 (01) : 193 - 205Scherer, Nora论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Spemann Grad Sch Biol & Med, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyFaessler, Daniel论文数: 0 引用数: 0 h-index: 0机构: Univ Med Greifswald, Dept Psychiat & Psychotherapy, Greifswald, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyBorisov, Oleg论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyCheng, Yurong论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanySchlosser, Pascal论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA Albert Ludwigs Univ Freiburg, Ctr Integrat Biol Signalling Studies, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany论文数: 引用数: h-index:机构:Haug, Stefan论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyLi, Yong论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyTelkaemper, Fabian论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Lab Clin Biochem & Metab, Adolescent Med & Neonatol Med Ctr, Fac Med Dept Gen Pediat, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyPatil, Suraj论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Spemann Grad Sch Biol & Med, Freiburg, Germany Univ Freiburg, Fac Med, Med Ctr, Dept Med Nephrol & Primary Care 4, Freiburg, Germany Univ Freiburg, Fac Biol, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyMeiselbach, Heike论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg, Univ Hosp Erlangen, Dept Nephrol & Hypertens, Erlangen, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyWong, Casper论文数: 0 引用数: 0 h-index: 0机构: Research, Maze Therapeut, South San Francisco, CA USA Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyBerger, Urs论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Lab Clin Biochem & Metab, Adolescent Med & Neonatol Med Ctr, Fac Med Dept Gen Pediat, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanySekula, Peggy论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyHoppmann, Anselm论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanySchultheiss, Ulla T.论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Univ Freiburg, Fac Med, Med Ctr, Dept Med Nephrol & Primary Care 4, Freiburg, Germany SYNLAB MVZ Humangenet Freiburg, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyMozaffari, Sahar论文数: 0 引用数: 0 h-index: 0机构: Research, Maze Therapeut, South San Francisco, CA USA Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyXi, Yannan论文数: 0 引用数: 0 h-index: 0机构: Research, Maze Therapeut, South San Francisco, CA USA Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyGraham, Robert论文数: 0 引用数: 0 h-index: 0机构: Research, Maze Therapeut, South San Francisco, CA USA Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanySchmidts, Miriam论文数: 0 引用数: 0 h-index: 0机构: Albert Ludwigs Univ Freiburg, Ctr Integrat Biol Signalling Studies, Freiburg, Germany Univ Freiburg, Fac Med, Med Ctr, Dept Gen Pediat Adolescent Med & Neonatol, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyKoettgen, Michael论文数: 0 引用数: 0 h-index: 0机构: Albert Ludwigs Univ Freiburg, Ctr Integrat Biol Signalling Studies, Freiburg, Germany Univ Freiburg, Fac Med, Med Ctr, Dept Med Nephrol & Primary Care 4, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyOefner, Peter J.论文数: 0 引用数: 0 h-index: 0机构: Univ Regensburg, Inst Funct Genom, Regensburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyKnauf, Felix论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Dept Nephrol & Intens Med Care, Berlin, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyEckardt, Kai-Uwe论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg, Univ Hosp Erlangen, Dept Nephrol & Hypertens, Erlangen, Germany Charite Univ Med Berlin, Dept Nephrol & Intens Med Care, Berlin, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyGruenert, Sarah C.论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Fac Med, Med Ctr, Dept Gen Pediat Adolescent Med & Neonatol, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyEstrada, Karol论文数: 0 引用数: 0 h-index: 0机构: Research, Maze Therapeut, South San Francisco, CA USA Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany论文数: 引用数: h-index:机构:Hertel, Johannes论文数: 0 引用数: 0 h-index: 0机构: Univ Med Greifswald, Dept Psychiat & Psychotherapy, Greifswald, Germany German Ctr Cardiovasc Res DZHK, Partner Site Greifswald, Greifswald, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, GermanyKoettgen, Anna论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany Univ Freiburg, Med Ctr, Freiburg, Germany Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA Albert Ludwigs Univ Freiburg, Ctr Integrat Biol Signalling Studies, Freiburg, Germany Univ Freiburg, Inst Genet Epidemiol, Fac Med, Freiburg, Germany